Clinical Research Associate (CRA)

About the Role

Our client is seeking a dedicated and meticulous Clinical Research Associate (CRA) to join their expanding clinical operations team in Coventry . In this crucial role, you will be responsible for ensuring the smooth and compliant execution of clinical trials at investigational sites. Your primary focus will be on monitoring site activities, verifying data integrity, and ensuring adherence to study protocols, regulatory requirements, and ethical standards, thereby playing a vital role in bringing new pharmaceutical products to market safely and effectively.

Key Responsibilities

• Conduct site visits (initiation, monitoring, close-out) according to the clinical trial protocol and regulatory guidelines.
• Verify the accuracy, completeness, and consistency of clinical data reported by investigational sites.
• Ensure compliance with study protocols, Good Clinical Practice (GCP) , and all applicable regulatory requirements.
• Build and maintain strong working relationships with investigators, site staff, and study sponsors.
• Identify and escalate any issues or deviations related to the trial conduct at the site level.
• Train site personnel on study-specific procedures and documentation requirements.

Requirements

• Bachelor's degree in a life science, nursing, or related field; advanced degree preferred.
• Proven experience as a Clinical Research Associate or in a similar clinical trial monitoring role.
• Thorough understanding of ICH-GCP guidelines and relevant regulatory requirements (e.g., FDA, EMA).
• Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
• Excellent organizational, problem-solving, and communication skills.
• Ability to travel frequently to investigational sites within the Coventry area and potentially beyond.

Benefits

• Competitive salary and performance-based incentives.
• Comprehensive benefits package including health, dental, and vision insurance.
• Generous paid time off and company holidays.
• Opportunities for career advancement and professional development within a growing organization.
• Supportive team environment focused on patient safety and data quality in clinical research.